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[关于鉴定Ⅰ型野生脊髓灰质炎病毒的快速检测策略研究]

[Study on the Fast Testing Strategy for identifying the wild poliovirus I].

作者信息

Gong Cheng, Luo Ming, Chen Meng, Zhang Tie-Gang, Zhang He-Run, Wang Yu-Mei, Li Ren-Qing, Dong Mei, Chen Wei-Xin, Chen Li-Juan

机构信息

The Immunization Institute, Beijing Center for Disease Control and Prevention, Beijing 100013, China.

出版信息

Zhonghua Liu Xing Bing Xue Za Zhi. 2012 Jul;33(7):726-9.

Abstract

OBJECTIVE

To explore the Fast Testing Sstrategy (FTS) for wild poliovirus I (WP1).

METHODS

Epidemiological investigations were carried out on 671 students from WP1 epidemic areas in China. A set of real time RT-PCR assays, including panenterovirus testings (PE) assay, poliovirus serotypings (PS) assay and the assay distinguishing wild strain from vaccine strain of poliovirus I (DWV) were introduced into the screening program for WPV1 to replace the conventional RT-PCR, recommended by the China National Polio Laboratory (GNPL). Additionally, sensitivities of all the assays were assessed by poliovirus type I to III (Sabin stain) and the isolated WPV1.

RESULTS

(1) 33 non-poliovirus enterovirus (NPEV) cases were detected, with 16 polio vaccine-related cases including 5 polio I, 1 polio II, 3 polio III, 1 polio I + II, 4 polio I + III and 2 polio I + II + III. Three WPV1 cases were also detected in this study and confirmed by CNPL. (2) For polio virus vaccine strain, sensitivities of the set of real time RT-PCR assays ranged from 1 to 100 times than that of the in-house RT-PCR assay. The sensitivities of PE and PS assays for the detection of polio II were 100 times than that of the RT-PCR assay and the sensitivity of DWV assay used for the detection of polio I were 10 times than that of the RT-PCR assay. For WPV1, the sensitivity of three real time RT-PCR was 10 times hight than that of the RT-PCR assay.

CONCLUSION

The novel FTS for WPV1 suggested by this study would include PE, PS and DWV. It not only could greatly shorten the testing time but also more sensitive than the RT-PCR and suited for emergency detection for WPV1.

摘要

目的

探索I型野生脊髓灰质炎病毒(WP1)的快速检测策略(FTS)。

方法

对来自中国WP1流行地区的671名学生进行了流行病学调查。将一组实时逆转录聚合酶链反应检测方法,包括肠道病毒通用检测(PE)试验、脊髓灰质炎病毒血清型鉴定(PS)试验以及区分I型脊髓灰质炎病毒野生株与疫苗株的检测(DWV)试验引入WPV1筛查程序,以取代中国国家脊髓灰质炎实验室(GNPL)推荐的传统逆转录聚合酶链反应。此外,用I至III型脊髓灰质炎病毒(萨宾株)和分离出的WPV1评估了所有检测方法的灵敏度。

结果

(1)检测到33例非脊髓灰质炎肠道病毒(NPEV)病例,其中16例与脊髓灰质炎疫苗相关,包括5例I型脊髓灰质炎、1例II型脊髓灰质炎、3例III型脊髓灰质炎、1例I + II型脊髓灰质炎、4例I + III型脊髓灰质炎和2例I + II + III型脊髓灰质炎。本研究还检测到3例WPV1病例,并经CNPL确认。(2)对于脊髓灰质炎病毒疫苗株,该组实时逆转录聚合酶链反应检测方法的灵敏度比内部逆转录聚合酶链反应检测方法高1至100倍。PE和PS试验检测II型脊髓灰质炎的灵敏度比逆转录聚合酶链反应检测方法高100倍,DWV试验检测I型脊髓灰质炎的灵敏度比逆转录聚合酶链反应检测方法高10倍。对于WPV1,三种实时逆转录聚合酶链反应的灵敏度比逆转录聚合酶链反应检测方法高10倍。

结论

本研究提出的新型WPV1 FTS将包括PE、PS和DWV。它不仅可以大大缩短检测时间,而且比逆转录聚合酶链反应更灵敏并且适合WPV1的应急检测。

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